A novel mutation in EXT2 gene in a Chinese family with hereditary multiple exostoses

Genet Test. 2008 Sep;12(3):331-2. doi: 10.1089/gte.2007.0124.

Abstract

Hereditary multiple exostoses (HME) is an autosomal-dominant disorder characterized by the presence of bony outgrowths on the long bones. In this report, we describe a Chinese family with HME. Linkage analysis and mutation detection were performed. Linkage with the EXT2 was established in this family. A novel mutation, EXT2 c239-244delG, was identified. Mutation analysis in a family with HME allows for genetic counseling and prenatal diagnosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics*
  • DNA Mutational Analysis
  • Exons
  • Exostoses, Multiple Hereditary / genetics*
  • Family
  • Female
  • Frameshift Mutation*
  • Gene Deletion
  • Genes*
  • Genetic Counseling
  • Genetic Linkage
  • Humans
  • Male
  • Pedigree
  • Phenotype